SLC67A1 Chromosome 11

Solute carrier family 67 member 1
1 variant 1 Health Risk

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What This Gene Does
This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015]
Gene Info
Gene Group
Solute carrier family 67
Locus Type
gene with protein product
Location
11p15.4
Ensembl
ENSG00000110628
Associated Conditions (3)
Rhabdomyosarcoma
somatic
SLC22A18-related disorder
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS78838117 Health Risk Conflicting classifications of pathogenicity Rhabdomyosarcoma, somatic, SLC22A18-related disorder
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